Senior Validation Engineer, L'Oréal Operations

L'Oréal; North Little Rock (AR); On-site; USD 110,000 - 140,000; Full time

Benefits offered by this job

Medical, Dental, Vision

401K

Pension Plan

Paid Holidays

Paid Vacation

Volunteer Time

Summer Fridays

VIP Shop discount

Monthly Mobile Allowance

Mentorship Programs

Job summary

L'Oréal North Little Rock seeks aSr. Engineer, Validation to lead CQV activities for equipment and processes in a regulated manufacturing environment. You will develop the MVP and draft IQ/OQ/PQ protocols while ensuring robust documentation and compliance.

Responsibilities include risk assessments, CAPA, change control, and cross-functional collaboration with Engineering, Production, Formulation, and QA. You will mentor junior staff and drive continuous improvement at a global beauty leader.

Qualifications

• Bachelor's degree in Chemical Engineering, Mechanical Engineering, Bioengineering, Chemistry, or related field.
• 5-7 years of manufacturing experience with CQV in cosmetics/pharma/personal care settings.
• Proven IQ/OQ/PQ protocol authoring and execution for equipment and utilities.
• Knowledge of GMP, ISO 22716, FDA and sanitary design principles.
• Strong statistical analysis and RCA skills for process validation.
• Experience validating automation systems (PLCs/SCADA) is desirable.
• Familiarity with cleaning validation, swab/rinse sampling, and analytical methods.
• Excellent technical writing, communication, and cross-functional leadership.
• Ability to mentor engineers and manage multiple validation projects.

Responsibilities

• Lead design, execution, and documentation of IQ/OQ/PQ protocols for equipment, lines, automation, and cleaning processes.
• Draft Master Validation Plan (MVP) and oversee validation studies.
• Manage risk assessments (FMEA), deviations, CAPA, and change control.
• Serve as site CQV expert for equipment and process validation activities.
• Mentor junior engineers and collaborate with Engineering, Production, Formulation, and QA.
• Ensure audit-ready documentation for regulatory inspections and client audits.
• Drive continuous improvement and re-validation as needed after changes.

Skills

CQV

IQ/OQ/PQ

GMP/ISO/FDA

statistical analysis

RCA

mentorship

cross-functional leadership

validation strategy

audit readiness

Education

Bachelor's degree in Chemical Engineering

Bachelor's degree in Mechanical Engineering

Bachelor's degree in Bioengineering

Bachelor's degree in Chemistry

Tools

PLCs

SCADA

Job description

Job Title: Sr Engineer, Validation
Location: North Little Rock, AR
Reports To: Manager - Quality Engineering
Who We Are: For more than a century, L'Oréal has devoted its energy, innovation, and scientific excellence solely to one business: Beauty. Our goal is to offer each and every person around the world the best of beauty in terms of quality, efficacy, safety, sincerity and responsibility to satisfy all beauty needs and desires in their infinite diversity.
At L'Oréal Operations, we create innovative, inclusive, and sustainable beauty together with our business partners by designing, developing, sourcing, manufacturing, and distributing over 6 billion products globally every year. We support over 36 brands across four L'Oréal divisions. We are consumer-oriented, and we act responsibly all along the value chain.

What You Will Do:

The Sr. Engineer of Validation is responsible for leading the design, execution, and documentation of validation protocols (IQ/OQ/PQ) for new and existing equipment, manufacturing lines, automation systems, and cleaning processes. This role brings robust technical expertise in commissioning, qualification, and validation (CQV) within a regulated environment, along with strong leadership skills to mentor junior engineers and drive continuous improvement across our production facility.

What We Are Looking For

• Bachelor's degree in Chemical Engineering, Mechanical Engineering, Bioengineering, Chemistry, or a related scientific/technical discipline required.
• 5-7 years of manufacturing experience (experience in commissioning, qualification, and validation (CQV) within the cosmetics, pharmaceutical, medical device, or personal care manufacturing industries preferred).
• Proven track record authoring and executing IQ/OQ/PQ protocols for manufacturing equipment (e.g., compounding vessels, filling lines, packaging equipment) and utility systems.
• Deep understanding of Good Manufacturing Practices (GMP), ISO 22716, FDA regulations, and sanitary design principles.
• Strong knowledge of statistical analysis tools and methodologies used in process validation.
• Experience with automation and control systems (PLCs, SCADA) validation is highly desirable.
• Familiarity with cleaning validation techniques, including swab/rinse sampling and analytical method parameters.
• Excellent technical writing skills with meticulous attention to detail and strong analytical, problem-solving, and root-cause analysis (RCA) capabilities.
• Effective communication and interpersonal skills, with the ability to lead cross-functional projects and mentor junior engineers and technicians.

Requirements

• Work independently to identify, investigate, and resolve validation deviations and implement sustainable CAPA solutions.
• Serve as the site expert for the deployment, commissioning, qualification, and validation (CQV) of equipment and processes.
• Possess an analytical mindset to synthesize complex validation data and statistical analysis into compliant technical plans.
• Resolve difficult technical and compliance issues on compounding, filling, packaging, and automated lines.
• Manage multiple validation projects simultaneously in a fast-paced, dynamic manufacturing environment.

The functions of Sr. Engineer, Validation include, but are not limited by the following:

• Validation Strategy & Planning: Develop and execute the Master Validation Plan (MVP) for the facility. Define validation requirements for new equipment installations, automated systems, manufacturing processes, and utility systems (water, compressed air, HVAC).
• Protocol Development & Execution: Draft, review, and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols. Ensure all testing aligns with internal quality standards and external regulatory requirements.
• Process & Cleaning Validation: Design and oversee process validation studies and cleaning validation programs to prevent cross-contamination and guarantee consistent product quality.
• Risk Management & Deviation Resolution: Conduct risk assessments (e.g., FMEA) to identify critical control points. Lead investigations into validation deviations, author comprehensive deviation reports, and implement robust Corrective and Preventive Actions (CAPA).
• Cross-Functional Collaboration: Partner closely with Engineering, Production, Formulation, and Quality Assurance teams to ensure seamless technology transfers, equipment commissioning, and process improvements.
• Change Control & Re-validation: Manage the validation impact of engineering change controls. Evaluate modifications to equipment, systems, or processes and determine the necessary re-validation requirements to maintain a qualified state.
• Audit Readiness & Compliance: Maintain all validation documentation in an audit-ready state. Serve as a subject matter expert (SME) during internal audits, client audits, and regulatory inspections (FDA, OSHA, ISO).
• Mentorship & Continuous Improvement: Provide guidance, training, and mentorship to junior validation engineers and technicians. Stay updated on industry trends, advancing technologies, and regulatory updates to continuously optimize validation methodologies.

What's In It For You

• Competitive Benefit Package (Medical, Dental, Vision, 401K, Pension Plan)
• Flexible Time Off (Paid Company Holidays, Paid Vacation, Vacation Buy Program, Volunteer Time, Summer Fridays & More!)
• Access to Company Perks (VIP Access to L'Oréal's Internal Shop for Discounted Products, Monthly Mobile Allowance)
• Learning & Development Opportunities (Unlimited Access to E-learnings, Lunch & Learn Sessions, Mentorship Programs, & More!)
• Employee Resource Groups (Think Tanks and Innovation Squads)
• Access to Mental Health & Wellness Programs

Don't meet every single requirement? At L'Oréal, we are dedicated to building a diverse, inclusive, and innovative workplace. If you're excited about this role but your past experience doesn't align perfectly with the qualifications listed in the job description, we encourage you to apply anyways! You may just be the right candidate for this or other roles!

We are an Equal Opportunity Employer and take pride in a diverse environment. We would love to find out more about you as a candidate and do not discriminate in recruitment, hiring, training, promotion, or other employment practices for reasons of race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status.